A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13560118



Internal ID3561934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93502909..93540123hg38UCSC Ensembl
chr9:96265191..96302405hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3837215
hg1937215
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621102
Supporting Variants
SamplesHG02060
Known GenesFAM120A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13560118
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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